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November 20–22, 2026 (Online)
What happens when a psychedelic protocol or study ends? This global virtual gathering unites patients, families, clinicians, researchers, and organizations across the field to examine emerging risks, unmet needs, and how lived experience can shape safer, more responsive care.
Understand this year’s timely theme and focus
9 roundtables, 3 synthesis panels + open community discussions
Meet the people shaping this year’s working summit
Our inaugural Psychedelic Lived Experiences Summit reached more than 3,000 attendees from 74 countries.
In November 2025, we brought together more than 60 patients, clinicians, and researchers across 54 in-depth interviews and 12 live panels to explore the benefits, limitations, and real-world complexities of psychedelic treatment. By uniting lived experience with scientific and clinical perspectives, the summit created the foundation we're building on in 2026.
DAYS
SPEAKERS
ATTENDEES
"The greatest resource we have for making progress in healthcare is the lived experience of those who are affected." – Dr. Lisa Sanders
Psychedelic treatments are often framed as breakthroughs, but real-world outcomes are far more complex, ranging from profound benefit to little change to lasting harm.
Clinical trials capture important measures, but lived experience reveals what those measures can miss: delayed risks, unexpected benefits and difficulties, everyday functioning, meaning, and the gap between protocol design and real life.
Yet as psychedelic research, care, and regulation evolve, the people who actually undergo these treatments still have too little influence over the decisions shaping them.
This is not a conference about patients. It is built and led by them, bringing lived experience into direct dialogue with research, practice, and ethical oversight to ask better questions, expose blind spots, and improve the decisions shaping psychedelic care.
2026 summit theme
Psychedelic treatment does not end when the session or study does. Benefits, risks, and destabilization can emerge long after formal follow-up ends, often beyond what research and care systems capture. In 2026, we focus on that gap: what happens next, what gets missed, and what better support, oversight, and accountability should look like.
Can’t attend live? Get all 2026 recordings plus last year’s 54 interviews and 12 panels.
Online | Nov 20-22, 2026
This summit is independently produced, with no grant, corporate, or pharma sponsorship. It is organized by people with firsthand experience of psychedelic clinical trials and treatments, creating space for lived experience to help set the agenda.
Join live and get six months of on-demand access to every session, so you can watch, revisit, and learn on your own time.
$119 USD
Full live and recording access to the 2026 summit, plus 2025 summit archive (54 interviews + 12 panels), workshop, and community spaces.
• 9 roundtables + 3 synthesis panels
• Recording of all 2026 sessions
• Complete 2025 summit archive
• 6 months of on-demand access
Pre-summit price: $119 USD through Nov 19 Regular price: $239 USD from Nov 20
$199 USD
Go beyond attending by helping make the summit possible for others while supporting the independent, lived experience work behind the summit.
• Everything included in Standard
• Helps fund full scholarship passes
• Supports free peer support circles
• Private gathering in Denver (2027)
Want to contribute more to our mission?
$299 USD → | $399 USD →
Via application
Full summit access for those who would otherwise be unable to attend due to cost. Limited number available.
• Everything included in Standard
• Open to patients, caregivers, students, and low-income attendees
• Priority for the Global South and other underrepresented regions
Pay-what-you-can scholarships opening soon via our newsletter
Meaningful progress cannot come from one group talking to itself. The 2026 summit is designed to bring different forms of expertise into the same room. Different perspectives will not always agree. That is precisely why they need to meet.
Patients and trial participants
People with diverse experiences of psychedelic clinical trials, treatments, and their longer-term consequences.
Family members and caregivers
Spouses, friends, colleagues, and other family members or caretakers of patients and trial participants.
Therapists, physicians, and nurses
Practitioners supporting screening, preparation, treatment, integration, recovery, and longer-term care.
Researchers and trial teams
Professionals designing studies, measuring outcomes, managing safety, and generating the field's evidence.
Ethics, policy, and advocacy
Those examining accountability, participant protection, access, regulation, and systemic change.
Organizations and field builders
Groups developing the infrastructure, communities, standards, and services surrounding psychedelic care.
Less presentation. More structured dialogue.
Each day features three facilitated 90-minute working roundtables followed by live synthesis discussions where invited contributors examine key questions through lived experience, research, clinical, and policy perspectives.
These discussions are designed to surface blind spots, identify priorities, and generate insights that can inform research, care, and future actions.
Summit attendees will watch the process unfold live and contribute through questions and participation opportunities.
Join the Psychedelic Lived Experiences Summit 2026 and help shape a shift toward safer, more responsive psychedelic care.
Live programming (Nov 20-22):
Can’t attend live?
Registration includes all 2026 recordings, plus last year’s full archive of 54 interviews and 12 live panels to watch later.
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Daily schedule |
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8:00am PST / 11:00am EST / 17:00 CET A focused 90-minute facilitated discussion bringing together lived experience and professional perspectives around one central question. |
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9:30am PST / 12:30pm EST / 18:30 CET The Zoom session will remain open for optional attendee discussion and reflection. Roundtable contributors may also join when available. |
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10:00am PST / 1:00pm EST / 19:00 CET A second in-depth working session examining another dimension of the day's theme. |
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11:30am PST / 2:30pm EST / 20:30 CET The Zoom session will remain open for optional attendee discussion and reflection. Roundtable contributors may also join when available. |
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12:00pm PST / 3:00pm EST / 21:00 CET A third collaborative session designed to surface gaps, tensions, lessons, and possible directions forward. |
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1:30pm PST / 4:30pm EST / 22:30 CET The Zoom session will remain open for optional attendee discussion and reflection. Roundtable contributors may also join when available. |
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2:00pm PST / 5:00pm EST / 23:00 CET Each day ends by identifying what emerged across the conversations: What did we learn? What remains unresolved? What happens next? |
What happens beyond the psychedelic protocol, from real-world outcomes and emerging risks to gaps in measurement, support, oversight, and accountability. Across MDMA, psilocybin, LSD, ketamine, 5-MeO-DMT, and ibogaine, we’ll examine why post-treatment care needs to extend beyond “integration” to include distinct layers of stabilization, safety monitoring, and continuity of care, informed by lived experience.
The final program is being developed with invited contributors and partner organizations. Topics under consideration include:
Post-protocol care: What happens to participants when structured support from treatment protocol or clinical research ends?
Ethics, accountability and oversight: Where do current safeguards work, where do they fail, and what needs to change?
Safety and emerging risk signals: What warning signs appear during the weeks and months following treatment, and which signals are currently missed?
Measuring what matters: Which outcomes should psychedelic research capture if we want to understand people's lives rather than only clinical endpoints?
Real-world outcomes: How do psychedelic experiences affect relationships, employment, identity, functioning, meaning, and quality of life beyond symptom scores?
Responsibility and continuity of care: What responsibilities do therapists, clinics, researchers, and institutions retain after the formal protocol ends?
Adverse events and challenging experiences: How should difficult outcomes be recognized, understood, documented, and responded to without minimizing or sensationalizing them?
Families, partners, and support networks: How are the people around psychedelic participants affected, and what role should they have in preparation and longer-term support?
Integration, stabilization, and longer-term recovery: What forms of peer or professional support are useful after favourable and/or destabilizing psychedelic experiences, and where are the existing gaps?
Lived experience in research and decision-making: How can patient and participant knowledge become a meaningful input into study design, clinical practice, safety systems, and policy?
The 2026 summit is designed to extend beyond the livestream by documenting questions, synthesizing insights, and identifying gaps, safety signals, research priorities, and areas for future collaboration. These findings may inform reports, recommendations, guidelines, or other public resources, turning dialogue into something the field can use.
Can’t attend live? Get all 2026 recordings plus last year’s 54 interviews and 12 panels.
Online | Nov 20-22, 2026
Live access Nov 20–22 + six months of recordings + the full 2025 archive.
Standard $119 | Supporter $199 | Scholarships available
More contributors will be announced over the coming weeks.
Psychedelic facilitator designing equitable pathways for psychedelic therapy within public healthcare systems, co-director at PMHA Alliance
Senior lecturer and psychedelic researcher at the University of Exeter’s EPIC, founder of Ripples, dedicated to peacebuilding
MDMA therapy clinical trial participant and caregiver to her husband after post-trial destabilization, award-winning author and resilience speaker
Psychologist, researcher, and clinician-scientist in psychotherapy at Humboldt-Universität zu Berlin, Germany
Clinical psychologist, founder and creator of ACER Integration, former psilocybin clinical lead at Imperial College London
U.S. veteran, founder and president of Heroic Hearts Project, a nonprofit supporting psychedelic therapy access for military veterans
Former Chief Scientific Officer at Resilient Pharmaceuticals (formerly Lykos/MAPS PBC), biologist, biotech leader, founder and CEO at Yazar Lab
Lawyer, psychedelic researcher, coach, peer support advocate, founder and executive director of Fireside Project
Phase 3 MDMA-assisted therapy for PTSD clinical trial participant (active arm), art therapist, peer support facilitator
Researcher and founder and CEO of the MIND Foundation, head of development at OVID Clinic in Berlin, Germany
Addiction psychiatrist and assistant professor at Yale School of Medicine researching psychedelics, substance use disorders, PTSD and neurobiology
MDMA-assisted psychotherapy for alcohol use disorder trial participant, trauma and recovery speaker and coach, creator of Design For Life
Psychologist and vice president at Mental Health America, focused on mental health equity, access, and inclusive systems of care
Lived Experience Council member at One Mind, director of lived experience at Motif Neurotech, co-founder at Otherside, mental health advocate
Professor of social work at Columbia University, health policy researcher, developer of psychedelic-assisted therapy training for social workers
Psychiatrist, psychedelic researcher, director of training at MGH’s Center for the Neuroscience of Psychedelics, Harvard Medical School faculty
Anthropologist, educator, author, speaker, activist, co-founder and executive director of the Chacruna Institute
CEO of TheraPsil, passionate advocate for legal, medical, and clinical access to psychedelic therapy for Canadians
Clinical psychologist and researcher dedicated to post-protocol safety, therapist training, and trauma-focused, ethical psychedelic care
Clinical psychologist, psychedelic scientist, and associate professor at the University of Wisconsin studying MDMA and psychedelics for addiction
Patient with lived experience of group ketamine-assisted psychotherapy and SPRAVATO® (esketamine) treatment for depression
Psychiatrist leading mood disorders research clinic in Newcastle, England, psychedelic trial principal investigator, lecturer, advisor, and educator
Former and founding CEO of Resilient Pharmaceuticals (Lykos/MAPS PBC), strategic advisor ensuring patient access to psychedelic therapies
U.S. army veteran, MDMA-assisted psychotherapy for PTSD clinical trial participant, music producer, mental health advocate
Senior manager of mental health equity and external partnerships for the national office of the Depression and Bipolar Support Alliance (DBSA)
Co-founder and CEO of Psychedelics Today, co-founder of Psychedelics and Pain Association nonprofit, breathwork facilitator
Phase 3 MDMA-assisted therapy for PTSD trial participant, advocate for trauma-informed healing, integration, and responsible storytelling
Clinical psychologist, psychedelic researcher, assistant professor at the University of Ottawa School of Psychology
Clinical research physician, former associate medical director at Resilient Pharmaceuticals (Lykos/MAPS PBC), quality assurance lead at Changemark
Psilocybin-assisted psychotherapy for life-threatening cancer through Canada’s Special Access Program, psychedelic therapy advocate
Emmy-winning user experience designer, One Mind Lived Experience Council member, IV ketamine and SPRAVATO® with therapy patient
Social scientist and psychedelic researcher focused on first-person inquiry at the University of Auckland, New Zealand
Psychiatric nurse practitioner, co-founder of OPENurses, clinician providing TMS and esketamine treatment in outpatient psychiatry
Phase 3 MDMA-assisted therapy for PTSD trial participant (placebo then crossover), ibogaine patient, peer supporter, and veterans advocate
Global drug safety advocate and speaker, consumer representative on an FDA advisory committee evaluating new drugs and patient safety
Author, journalist and facilitator, executive director of the Breaking Convention, a UK conference on psychedelic medicine and culture
Associate professor of philosophy and bioethics at SUNY Upstate Medical University, author of Reclaiming the Self in Psychiatry
Founder, CEO, and board chair of the National Psychedelics Association, supporting professionals working in psychedelic-assisted care
Executive director of the Healing Advocacy Fund, supporting access to psychedelic therapies through state-regulated programs
Neuropharmacologist, psychedelic researcher and educator, co-founder of Psychedelic Support, scientific advisor to psychedelic nonprofits
Phase 3 MDMA-assisted therapy for PTSD clinical trial participant (placebo only), mental health and psychedelic participant rights advocate
Biotech leader focused on patient strategy at AtaiBeckley, strategy consultant at Amandala Neuro, previously with Johnson & Johnson
Art therapy student, ACER Integration facilitator, client care at FlowState Therapy ketamine clinic, caregiver and family support advocate
Faculty for Yale School of Medicine's Lived Experience Transformational Leadership Academy, former director of operations at the Fireside Project
Registered nurse specializing in emergency nursing and ketamine-assisted therapy for mental health conditions and chronic pain
Family and sports medicine physician, president of the Psychedelic Medicine Association, and host of the Psychedelic Medicine Podcast
Founder and executive director of the Psychedelic Medicine Coalition, advocate for federal psychedelic policy, access, and education
Psychoactive substance for PTSD Phase 2 clinical trial participant (double blinded then open label), mental health counsellor
Facilitating the summit’s working sessions and helping guide focused, multi-stakeholder dialogue. More moderators will be announced over the coming weeks.
Community strategist and consultant, trained psychedelic peer support facilitator, focused on participatory communities, harm reduction, and public education
Emergency medicine physician, anesthesiologist, neuroscientist, and researcher specializing in psychedelic medicine, adjunct professor at the University of Ottawa
Chartered psychologist and head of research at Drug Science, honorary senior fellow at UK's Imperial and King’s, focused on psychedelics, real world data, ethics, and patient access
Psychotherapist, clinical social worker, psychedelic educator, and harm reduction specialist focused on integration, practitioner education, and mental health care
Executive director of Zendo Project, licensed therapist and psychedelic harm reduction practitioner with extensive experience in peer support and crisis response
Senior director at BrainFutures, leading U.S. national initiatives on psychedelic therapy access, clinical integration, policy, and mental health system implementation
Integrative psychotherapist specializing in trauma, IFS, and psychedelic-assisted therapy across ketamine, psilocybin clinical trials, and Canada’s Special Access Program
Additional moderator selected to help facilitate the roundtable discussion and contribute relevant perspective and expertise. Full details will be announced soon.
Additional moderator selected to help facilitate the roundtable discussion and contribute relevant perspective and expertise. Full details will be announced soon.
Hi, I'm Pedram Dara, a former MDMA-assisted therapy clinical trial participant and founder and director of the Psychedelic Lived Experiences, a patient-led initiative strengthening decision-making by bringing lived experience and clinical science together for safer, more ethical psychedelic research, care, and policy.
Since 2019, I’ve advocated for patient safety and treatment efficacy, speaking at major forums such as the European Parliament and the FDA, and at leading conferences like Psychedelic Science, ICPR, and International Trauma Conference. My story and insights are featured in news, documentaries, training programs, research projects, and journal publications.
I believe true progress in psychedelics care requires moving beyond hype and fear to embrace the depth, complexity, and wisdom of those who’ve lived it.
"Research leads to meaningful healing when it’s done with people, not just on them. When lived experience informs how studies are designed, conducted, and understood, research becomes more than data generation, it becomes a compass for healthcare transformation." – Pedram Dara
Join patients, families, clinicians, researchers, advocates, and organizations from around the world to explore what happens when psychedelic treatment ends and real life continues. Together, we’ll examine what we know, what we’re missing, and what safer, more responsive care requires.
Can’t attend live? Get all 2026 recordings plus last year’s 54 interviews and 12 panels.
Online | Nov 20-22, 2026
Share this event with your network and join together in shaping the future of patient-centered psychedelic care.
This summit is independently produced, with no grant, corporate, or pharma sponsorship. It is organized by people with firsthand experience of psychedelic clinical trials and treatments, creating space for lived experience to help set the agenda.
Join live and get six months of on-demand access to every session, so you can watch, revisit, and learn on your own time.
$119 USD
Full live and recording access to the 2026 summit, plus 2025 summit archive (54 interviews + 12 panels), workshop, and community spaces.
• 9 roundtables + 3 synthesis panels
• Recording of all 2026 sessions
• Complete 2025 summit archive
• 6 months of on-demand access
Pre-summit price: $119 USD through Nov 19 Regular price: $239 USD from Nov 20
$199 USD
Go beyond attending by helping make the summit possible for others while supporting the independent, lived experience work behind the summit.
• Everything included in Standard
• Helps fund full scholarship passes
• Supports free peer support circles
• Private gathering in Denver (2027)
Want to contribute more to our mission?
$299 USD → | $399 USD →
Via application
Full summit access for those who would otherwise be unable to attend due to cost. Limited number available.
• Everything included in Standard
• Open to patients, caregivers, students, and low-income attendees
• Priority for the Global South and other underrepresented regions
Pay-what-you-can scholarships opening soon via our newsletter
The 2025 archive features 54 conversations and 12 live panels with 27 patients and trial participants alongside 27 therapists and researchers, exploring benefits, challenges, safety, integration, ethics, research gaps, and the unique complexities of psychedelic treatment. 2026 access options will include the archive alongside this year’s new program.
Former patients and trial participants in treatments with MDMA, Psilocybin, LSD, Ketamine, 5-MeO-DMT, Ibogaine and other psychoactive substances offer powerful insights to improve research design, therapist training, and future treatment outcomes.
MDMA-assisted therapy for PTSD, special access program patient (Canada, 2024)
MDMA-assisted psychotherapy for PTSD, Phase 3 trial participant (active arm, U.S., 2021)
Ibogaine & 5-MeO-DMT for PTSD, anxiety, & addiction, clinical treatment patient (Mexico/U.S. 2022-23)
Ibogaine for opioid dependency, clinical treatment patient & therapist (U.S. 2011)
Psilocybin for depression pilot study and phase 2 clinical trials participant (UK, 2015 and 2019)
Psilocybin-assisted therapy for anorexia nervosa, Phase 1 trial participant (open-label, U.S., 2021)
U.S. veteran, peer support and study facilitator for MDMA and psilocybin studies (U.S.)
Psilocybin for treatment-resistant depression, clinical trial participant (open-label, Canada, 2022)
Group ketamine therapy & SPRAVATO® (esketamine) for depression, treatment patient (U.S., 2025)
Psilocybin and DMT for depression clinical trials participant (UK, 2019 and 2022)
Ketamine therapy for bipolar I, depression, and anxiety, clinical treatment patient (U.S., 2022)
Psilocybin for treatment-resistant depression, Phase 2 clinical trial participant (UK, 2021)
LSD-assisted therapy for life-threatening illness, compassionate use patient (Switzerland, 2020)
Legal psilocybin retreat for terminal cancer participant, psychiatrist, trial doctor & therapist (UK, 2018)
SPRAVATO® (esketamine) for depression, clinical treatment patient (Belgium, 2022)
Psilocybin-assisted therapy for terminal cancer, special access program patient (Canada, 2021)
MDMA-assisted therapy for PTSD, Phase 3 trial participant (placebo then crossover, U.S., 2023)
Ketamine, MDMA, LSD, and Psilocybin for experiential therapist training study (Switzerland, 2025)
MDMA-assisted therapy in experiential training for a police officer-therapist (U.S., 2018)
MDMA-assisted therapy for PTSD, Phase 3 trial participant (placebo only, U.S., 2021)
MDMA-assisted psychotherapy for PTSD, Phase 3 trial participant (active arm, U.S., 2020)
Psilocybin-assisted therapy for generalized anxiety disorder, clinical trial participant (Australia, 2022)
Psychoactive substance for PTSD Phase 2 clinical trial participant (double blinded then open label, UK, 2024)
Psilocybin-assisted therapy for advanced cancer trial participant, registered therapist (Canada, 2025)
MDMA-assisted massed exposure therapy for PTSD, Phase 2 trial participant (open-label, U.S., 2025)
Psilocybin for treatment-resistant depression, clinical trial participant (open-label, Canada, 2022)
MDMA and LSD assisted therapies for depression, compassionate use patient (Switzerland, 2022)
Leading clinicians and researchers in psychedelic science share insights on integrating lived experience to improve clinical trials, therapist training, and treatment outcomes.
NOTE: Speakers featured for expertise only; views/actions aren’t endorsed. Learn more ->
Psychiatrist, author of The Body Keeps the Score, and principal investigator for MDMA-assisted therapy for PTSD trials (U.S.)
Clinical psychologist, ACER Integration founder, and former psilocybin clinical lead at Imperial College London (UK)
Psychiatrist, clinical researcher, and medical monitor for MDMA-assisted psychotherapy for PTSD clinical trials (U.S.)
Therapist, lead trainer, supervisor, and principal investigator for MDMA-assisted therapy for PTSD clinical trials (U.S.)
Therapist, lead trainer, supervisor, and sub-investigator for MDMA-assisted therapy for PTSD clinical trials (U.S.)
Pediatrician, researcher, former Chief Medical Officer at Lykos/MAPS PBC, and founder & CEO at Tulip Medical Consulting (U.S.)
Psychedelic researcher, experimental psychologist, senior investigator, and professor at Johns Hopkins School of Medicine (U.S.)
Clinical psychologist, researcher, and professor in the school of psychology at University of Ottawa (Canada)
Psychologist, renowned Ibogaine expert, published researcher, and CEO & co-founder at Ambio Life Sciences (Mexico/Canada)
Clinical psychologist, founder and director of the CIIS Center for Psychedelic Therapies and Research (U.S.)
Psychiatrist, psilocybin clinical researcher, and associate professor at Johns Hopkins University (U.S.)
Marriage and family therapist, lead psychedelic clinical trial therapist at Imperial College London (UK)
Psychologist, clinical researcher and head of Clinical Psychedelic Lab at Monash University (Australia)
Family physician and therapeutic counsellor, investigator for Phase 3 MDMA-assisted therapy for PTSD trials (Canada)
Neuroscientist, researcher at UCSF working with Robin Carhart-Harris, PhD on the impact of psychedelics on mental health (U.S.)
Psychiatrist and clinical researcher for MDMA therapy for PTSD and psilocybin for advanced cancer trials (Canada)
Psychiatrist and addiction medicine specialist, group MDMA therapy investigator for veterans with PTSD (U.S.)
Psychiatrist, research psychologist with PhD in ayahuasca and mental health, lecturer at the University of Exeter (UK)
Qualitative researcher in psychedelic trials and executive director of the OPEN Foundation (Netherlands)
Physician, board member of the Psychedelic Association of Canada and medical lead at the Roots to Thrive (Canada)
Palliative care physician and psychedelic therapist specializing in psilocybin therapy for terminal illness (Canada)
Psychiatrist, psychedelic therapist, and founder of the Compassionate Care Center in Geneva (Switzerland)
Psychiatrist, investigator for MDMA therapy for PTSD trials (Canada) and psilocybin for anxiety trials (Australia)
Therapist specializing in medicine assisted therapy, clinic director & co-founder at Centre for Medicine Assisted Therapy (Canada)
Psychologist, clinical researcher, psychedelic educator, author, and supervisor to therapists on clinical trials (U.S.)
Psychiatry resident and lead author on Delphi study for reporting of setting in psychedelic trials (Canada)
Clinical psychologist and qualitative researcher in MDMA therapy for terminal illness and studies with psilocybin & ketamine (U.S.)
Join patients, families, clinicians, researchers, advocates, and organizations from around the world to explore what happens when psychedelic treatment ends and real life continues. Together, we’ll examine what we know, what we’re missing, and what safer, more responsive care requires.
Can’t attend live? Get all 2026 recordings plus last year’s 54 interviews and 12 panels.
Online | Nov 20-22, 2026
Share this event with your network and join together in shaping the future of patient-centered psychedelic care.
The Psychedelic Lived Experiences Summit runs from November 20th to November 22nd, 2026. Live programming: 11:00 AM–6:00 PM EST / 8:00 AM–3:00 PM PST / 5:00 PM–12:00 AM CET
Yes, all sessions will be recorded. You'll get unlimited 1-year access to all the recordings, plus other exclusive perks we'll announce soon.
If you’ve checked all your inbox folders (including spam, junk, and promotions) and still don’t see the email, please reach out to us. We’re happy to help! >>> contact@psychedeliclivedexperiences.com